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IFT172 Antibodies

AND IFT172 ELISA kits, IFT172 Proteins

Many biological assays use antibodies to detect IFT172, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with IFT172 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop IFT172 antibodies...

We validate the specificity of these antibodies to IFT172 by testing them on tissues known to express IFT172 positively and negatively. Browse below to find the IFT172 antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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IFT172 Infographic by Boster Bio

IFT172 protein infographic

All IFT172 Products

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Anti-IFT172 Antibody Picoband®

Human, Mouse, Rat

ELISA, WB

$370
Cat # A08217-1
100 µg/vial

IFT172 Overview

Facts about Intraflagellar transport protein 172 homolog.

IFT172 3D structure

IFT172 3D structure. Source: alphafold

Intraflagellar transport protein 172 homolog (IFT172)

Required for the maintenance and formation of cilia. Plays an indirect role in hedgehog (Hh) signaling, cilia needing all activity of the hedgehog pathway (By similarity).

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Gene Information

Human
Gene Name:	IFT172
Uniprot:	Q9UG01
Entrez:	26160

Gene Information

Family

Belongs to:

IFT172 family

Family

Alternative Names

DKFZp434A163; intraflagellar transport 172 homolog (Chlamydomonas); intraflagellar transport protein 172 homolog

Molecular Weight

Mass (kDA):
197.576 kDA

Molecular Weight

Genomic Context


Human

Location:	2p23.3
Sequence:	2; NC_000002.12 (27444373..27489819, complement)

Subcellular Localizations

Cell projection, cilium. Localized to the axoneme and around the base of the cilium.

Subcellular Localization

Diseases

Limb Deformities, Congenital
Hereditary Diseases
Polycystic Kidney Diseases
Kidney Diseases
Retinal Degeneration
Kartagener Syndrome
Polydactyly
Bardet-biedl Syndrome
Cystic Kidney Diseases
Diabetes Mellitus
Hydrocephalus
Holoprosencephaly
Hypokinesia

Polycystic Kidney, Autosomal Dominant
Hypertensive Disease
Congenital Heart Defects
Edema
Vacterl Association
Endocardial Cushion Defects
Obesity

Disease

Pathways

Transport
Intraflagellar Transport
Localization
Gastrulation
Spinal Cord Patterning
Fertilization
Pathogenesis

Rna Interference

Pathways

PTMs

Acetylation
Isopeptide bond

Methylation
Ubl conjugation

Bosterbio | ELISA Kits, Antibodies, Antibody Company

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/IFT172

References

PMID: 20388717 by Blomster H.A., et al. In vivo identification of sumoylation sites by a signature tag and cysteine-targeted affinity purification.

PMID: 24140113 by Halbritter J., et al. Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans.